A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4217



Internal ID15538944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:62494615..62517842hg38UCSC Ensembl
Outerchr16:62528519..62551746hg19UCSC Ensembl
Outerchr16:61086020..61109247hg18UCSC Ensembl
Outerchr16:61086020..61109247hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3823228
hg1923228
hg1823228
hg1723228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1826
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv4217
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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